HU198512B - Process for producing peptide with anticoagulant effect and pharmaceutical composition comprising same - Google Patents
Process for producing peptide with anticoagulant effect and pharmaceutical composition comprising same Download PDFInfo
- Publication number
- HU198512B HU198512B HU882615A HU261588A HU198512B HU 198512 B HU198512 B HU 198512B HU 882615 A HU882615 A HU 882615A HU 261588 A HU261588 A HU 261588A HU 198512 B HU198512 B HU 198512B
- Authority
- HU
- Hungary
- Prior art keywords
- peptide
- group
- glu
- pharmaceutical composition
- amino acid
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- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 235000014705 isoleucine Nutrition 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 208000010125 myocardial infarction Diseases 0.000 description 1
- 210000004165 myocardium Anatomy 0.000 description 1
- ADAMEOZKZQRNKP-UHFFFAOYSA-N n'-propylmethanediimine Chemical compound CCCN=C=N ADAMEOZKZQRNKP-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 238000005897 peptide coupling reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 210000003079 salivary gland Anatomy 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/64—Cyclic peptides containing only normal peptide links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/81—Protease inhibitors
- C07K14/815—Protease inhibitors from leeches, e.g. hirudin, eglin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Tropical Medicine & Parasitology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5320487A | 1987-05-21 | 1987-05-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HUT47136A HUT47136A (en) | 1989-01-30 |
| HU198512B true HU198512B (en) | 1989-10-30 |
Family
ID=21982612
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU882615A HU198512B (en) | 1987-05-21 | 1988-05-20 | Process for producing peptide with anticoagulant effect and pharmaceutical composition comprising same |
Country Status (17)
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5192745A (en) * | 1987-05-21 | 1993-03-09 | Merrell Dow Pharmaceuticals Inc. | Cyclic anticoagulant peptides |
| US5236898A (en) * | 1987-05-21 | 1993-08-17 | Merrell Dow Pharmaceuticals Inc. | Cyclic anticoagulant peptides |
| CA1328540C (en) * | 1987-05-21 | 1994-04-12 | John L. Krstenansky | Cyclic anticoagulant peptides |
| NZ228995A (en) * | 1988-05-10 | 1992-03-26 | Merrell Dow Pharma | Hirudin peptide derivatives and pharmaceutical compositions |
| US5196404B1 (en) * | 1989-08-18 | 1996-09-10 | Biogen Inc | Inhibitors of thrombin |
| US5240913A (en) * | 1989-08-18 | 1993-08-31 | Biogen, Inc. | Inhibitors of thrombin |
| US5192747A (en) * | 1989-10-03 | 1993-03-09 | Merrell Dow Pharmaceuticals Inc. | Anticoagulant peptides |
| CA2026377A1 (en) * | 1989-10-03 | 1991-04-04 | John L. Krstenansky | Radiolabeled anticoagulant peptides |
| CA2035917C (en) * | 1990-02-13 | 2001-10-02 | John L. Krstenansky | Stabilized sulfonate, sulfate, phosphonate and phosphate derivatives of hirudin |
| US5242810A (en) * | 1990-12-07 | 1993-09-07 | Biogen, Inc. | Bifunctional inhibitors of thrombin and platelet activation |
| DE4103649A1 (de) * | 1991-02-07 | 1992-08-13 | Basf Ag | Neue antikoagulatorisch wirksame peptide |
| US5516889A (en) * | 1993-06-21 | 1996-05-14 | University Technologies International, Inc. | Synthetic thrombin receptor peptides |
| ES2305819T3 (es) | 2003-08-08 | 2008-11-01 | Westfalia Separator Gmbh | Separador que tiene un tambor de centrifugado con un paquete de discos. |
| CN104054441A (zh) * | 2014-06-30 | 2014-09-24 | 泰州樱田农机制造有限公司 | 撒肥机排料调节装置 |
| CN110981953B (zh) * | 2019-12-13 | 2021-10-08 | 首都医科大学 | 一种多肽和多肽的应用及包含多肽的组合物 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1328540C (en) * | 1987-05-21 | 1994-04-12 | John L. Krstenansky | Cyclic anticoagulant peptides |
-
1988
- 1988-05-16 CA CA000566915A patent/CA1328540C/en not_active Expired - Fee Related
- 1988-05-16 ZA ZA883444A patent/ZA883444B/xx unknown
- 1988-05-17 AU AU16343/88A patent/AU608846B2/en not_active Ceased
- 1988-05-18 NZ NZ224677A patent/NZ224677A/xx unknown
- 1988-05-19 FI FI882359A patent/FI89064C/fi not_active IP Right Cessation
- 1988-05-19 ES ES88108047T patent/ES2054732T3/es not_active Expired - Lifetime
- 1988-05-19 EP EP88108047A patent/EP0291981B1/en not_active Expired - Lifetime
- 1988-05-19 KR KR1019880005871A patent/KR880013977A/ko not_active Ceased
- 1988-05-19 IL IL86439A patent/IL86439A/xx unknown
- 1988-05-19 AT AT88108047T patent/ATE88190T1/de active
- 1988-05-19 PT PT87537A patent/PT87537B/pt not_active IP Right Cessation
- 1988-05-19 DE DE8888108047T patent/DE3880194T2/de not_active Expired - Fee Related
- 1988-05-20 JP JP63122189A patent/JP2598302B2/ja not_active Expired - Fee Related
- 1988-05-20 NO NO882239A patent/NO882239L/no unknown
- 1988-05-20 DK DK278588A patent/DK278588A/da not_active Application Discontinuation
- 1988-05-20 HU HU882615A patent/HU198512B/hu not_active IP Right Cessation
- 1988-05-21 CN CN198888103009A patent/CN88103009A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FI882359A0 (fi) | 1988-05-19 |
| NO882239L (no) | 1988-11-22 |
| JPS63307895A (ja) | 1988-12-15 |
| ATE88190T1 (de) | 1993-04-15 |
| KR880013977A (ko) | 1988-12-22 |
| JP2598302B2 (ja) | 1997-04-09 |
| ZA883444B (enrdf_load_stackoverflow) | 1988-11-16 |
| EP0291981A3 (en) | 1990-07-04 |
| DE3880194T2 (de) | 1993-08-26 |
| CA1328540C (en) | 1994-04-12 |
| HUT47136A (en) | 1989-01-30 |
| ES2054732T3 (es) | 1994-08-16 |
| PT87537B (pt) | 1992-09-30 |
| CN88103009A (zh) | 1988-12-21 |
| FI89064B (fi) | 1993-04-30 |
| IL86439A (en) | 1992-11-15 |
| FI89064C (fi) | 1993-08-10 |
| NO882239D0 (no) | 1988-05-20 |
| DK278588A (da) | 1988-11-22 |
| FI882359A7 (fi) | 1988-11-22 |
| EP0291981A2 (en) | 1988-11-23 |
| NZ224677A (en) | 1990-08-28 |
| DK278588D0 (da) | 1988-05-20 |
| IL86439A0 (en) | 1988-11-15 |
| AU1634388A (en) | 1988-11-24 |
| DE3880194D1 (de) | 1993-05-19 |
| PT87537A (pt) | 1989-05-31 |
| EP0291981B1 (en) | 1993-04-14 |
| AU608846B2 (en) | 1991-04-18 |
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| DE69032258T2 (de) | Antikoagulierende Peptide | |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |